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Tyrosine Hydroxylase (PTR2544) Mouse mAb

-YM33070

Catalog: YM33070
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$160.00
In stock

0

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Main Information
Target

Tyrosine Hydroxylase

Host Species

Mouse

Reactivity

Human, Mouse, Rat,

Applications

WB, IF, ELISA

MW

58kD (Calculated)

59kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-2000; IF 1:100-500; ELISA 1:1000-5000
Formulation
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Specificity
This antibody detects endogenous levels of Tyrosine Hydroxylase protein.
Purification
Protein G
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
1 mg/ml
MW(Calculated)
58kD
MW(Observed)
59kD
Modification
Unmodified
Clonality
Monoclonal
Clone Number
PTR2544
Isotype
IgG1,Kappa
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Antigen&Target Information
Immunogen:
Synthesized peptide derived from human Tyrosine Hydrolase AA range: 1-100
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Specificity:
This antibody detects endogenous levels of Tyrosine Hydroxylase protein.
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Gene Name:
TH TYH
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Protein Name:
Tyrosine 3-monooxygenase (Tyrosine 3-hydroxylase) (TH),Tyrosine Hydrolase
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Other Name:
Tyrosine 3-monooxygenase ;
Tyrosine 3-hydroxylase ;
TH ;
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Database Link:
Organism Gene ID SwissProt
Human 7054; P07101;
Mouse 21823; P24529;
Rat 25085; P04177;
Background:
The protein encoded by this gene is involved in the conversion of tyrosine to dopamine. It is the rate-limiting enzyme in the synthesis of catecholamines, hence plays a key role in the physiology of adrenergic neurons. Mutations in this gene have been associated with autosomal recessive Segawa syndrome. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008],
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Function:
Catalytic activity:L-tyrosine + tetrahydrobiopterin + O(2) = 3,4-dihydroxy-L-phenylalanine + 4a-hydroxytetrahydrobiopterin.,cofactor:Fe(2+) ion.,Disease:Defects in TH are the cause of dystonia DOPA-responsive autosomal recessive (ARDRD) [MIM:605407]; also known as autosomal recessive Segawa syndrome. ARDRD is a form of DOPA-responsive dystonia presenting in infancy or early childhood. Dystonia is defined by the presence of sustained involuntary muscle contractions, often leading to abnormal postures. Some cases of ARDRD present with parkinsonian symptoms in infancy. Unlike all other forms of dystonia, it is an eminently treatable condition, due to a favorable response to L-DOPA.,enzyme regulation:Phosphorylation leads to an increase in the catalytic activity.,Function:Plays an important role in the physiology of adrenergic neurons.,online information:Tyrosine hydroxylase entry,pathway:Catecholamine biosynthesis; dopamine biosynthesis; dopamine from L-tyrosine: step 1/2.,similarity:Belongs to the biopterin-dependent aromatic amino acid hydroxylase family.,tissue specificity:Mainly expressed in the brain and adrenal glands.,
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Tissue Expression:
Mainly expressed in the brain and adrenal glands.
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Research Areas:
>>Tyrosine metabolism ;
>>Folate biosynthesis ;
>>Metabolic pathways ;
>>Dopaminergic synapse ;
>>Prolactin signaling pathway ;
>>Parkinson disease ;
>>Cocaine addiction ;
>>Amphetamine addiction ;
>>Alcoholism
show all
Catalog: YM33070
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$160.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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